Canonical Allele Identifier: CA339321219
Gene: GJA4 HGNC NCBI
SMIM12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.35259962T>A (hg19) chr1:g.34794361T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34794361T>A , CM000663.2:g.34794361T>A GRCh38
NC_000001.10:g.35259962T>A , CM000663.1:g.35259962T>A GRCh37
NC_000001.9:g.35032549T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000342280.5:c.148T>A (GJA4) MANE Select ENSP00000343676.4:p.Ser50Thr
ENST00000342280.4:c.148T>A (GJA4) ENSP00000343676.4:p.Ser50Thr
ENST00000426886.1:c.207+61410A>T (SMIM12) ENSP00000429902.1:n.207+61410A>T
ENST00000450137.1:c.148T>A (GJA4) ENSP00000409186.1:p.Ser50Thr
NM_002060.2:c.148T>A (GJA4) NP_002051.2:p.Ser50Thr
XM_005270750.1:c.148T>A (GJA4) XP_005270807.1:p.Ser50Thr
XR_947179.1:n.1001+4010A>T
XM_005270750.2:c.148T>A (GJA4) XP_005270807.1:p.Ser50Thr
XM_017001043.2:c.148T>A (GJA4) XP_016856532.1:p.Ser50Thr
XR_001737967.1:n.1023+4010A>T
NM_002060.3:c.148T>A (GJA4) MANE Select NP_002051.2:p.Ser50Thr
Search 100 bp 5'
Search 100 bp 3'